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dc.contributor.authorGarcía Rubiño, María Eugenia
dc.contributor.authorMatilla Hernández, Antonio
dc.contributor.authorFrontera, Antonio
dc.contributor.authorLezama Diago, Luis María
dc.contributor.authorNiclós Gutiérrez, Juan
dc.contributor.authorChoquesillo Lazarte, Duane
dc.date.accessioned2021-05-27T12:15:03Z
dc.date.available2021-05-27T12:15:03Z
dc.date.issued2021-05-02
dc.identifier.citationPharmaceuticals 14(5) : (2021) // Article ID 426es_ES
dc.identifier.issn1424-8247
dc.identifier.urihttp://hdl.handle.net/10810/51649
dc.description.abstractIn the extensive field of metal ions, their interactions with nucleic acids, and their constituents, the main aim of this work is to develop a metal chelate suitable to recognize two molecules of an adenine nucleoside. For this purpose, the dinuclear chelate Cu2 (µ-EDTA) (ethylenediaminetetraacetate(4-) ion (EDTA)) is chosen as a bicephalic receptor model for N9-(2-hydroxyethyl)adenine (9heade). A one-pot synthesis is reported to obtain the compound [Cu2(µ2-EDTA)(9heade)2(H2O)4]·3H2O, which has been characterized by single-crystal X-ray diffraction and various spectral, thermal, and magnetic methods. The complex unit is a centro-symmetric molecule, where each Cu (II) center is chelated by a half-EDTA, and is further surrounded by an N7-dentate 9heade nucleoside and two non-equivalent trans-O-aqua molecules. The metal chelate-nucleoside molecular recognition is referred to as an efficient cooperation between the Cu-N7(9heade) coordination bond and a (9heade)N6-H···O(carboxyl, EDTA) interligand interaction. Theoretical calculations are also made to account for the relevance of this interaction. The extreme weakness with which each water molecule binds to the metal center disturbs the thermal stability and the infrared (FT-IR) and electron spin resonance (ESR) spectra of the compound.es_ES
dc.description.sponsorshipThis research was funded by Agencia Estatal de Investigación, Ministerio de Ciencia, Innovación y Universidades (MICIU) from Spain, and was co-funded by FEDER-EU (project nos. PGC2018-102047-B-I00 and CTQ2017-85821-R), Junta de Andalucía (research group FQM-283), and University of Granada (project ref. PPJIA2019-03).es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MCIU/PGC2018-102047-B-I00es_ES
dc.relationinfo:eu-repo/grantAgreement/MCIU/CTQ2017-85821-Res_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjectadeninees_ES
dc.subjectsynthetic nucleosidees_ES
dc.subjectmodel receptores_ES
dc.subjectcopperes_ES
dc.subjectbicephalic chelatees_ES
dc.titleDicopper(II)-EDTA Chelate as a Bicephalic Receptor Model for a Synthetic Adenine Nucleosidees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2021-05-24T15:06:33Z
dc.rights.holder2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1424-8247/14/5/426/htmes_ES
dc.identifier.doi10.3390/ph14050426
dc.departamentoesQuímica Orgánica e Inorgánica
dc.departamentoeuKimika Organikoa eta Ez-Organikoa


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2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).